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Aldehydes and ketones influence reactivity and selectivity in nickel-catalysed Suzuki–Miyaura reactions

The energetically-favorable coordination of aldehydes and ketones – but not esters or amides – to Ni(0) during Suzuki–Miyaura reactions can lead either to exquisite selectivity and enhanced reactivity, or to inhibition of the reaction. Aryl halides where the C–X bond is connected to the same π-syste...

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Detalles Bibliográficos
Autores principales: Cooper, Alasdair K., Leonard, David K., Bajo, Sonia, Burton, Paul M., Nelson, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148322/
https://www.ncbi.nlm.nih.gov/pubmed/34123283
http://dx.doi.org/10.1039/c9sc05444h

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